Ovarian Cancer and Mutation 5382insC in BRCA1 Gene (Clinical Case)
Journal: Archive of Clinical Medicine (Vol.21, No. 2)Publication Date: 2015-12-31
Authors : O. V. Paliychuk; Z. I. Rossokha;
Page : 19-22
Keywords : genealogic tree; proband; familial cancer syndrome; mutations in BRCA1/2 genes; ovarian cancer; breast cancer;
Abstract
Case report was described and familial cancer syndrome in proband’s family was established. Based on the results of complex examination and medical-genetic counseling proband’s disease was associated with mutation 5382 insС in BRCA1 gene indicating the role of molecular genetic testing for timely detection of malignant ovarian and breast pathology in families with burdened history of cancer.
Other Latest Articles
- Hemochromatosis and Hemosiderosis in Children
- Effectiveness of Complex Treatment of Patients with Chronic Heart Failure Taking into Account Immune System Condition
- Study of Foreign Students’ Attitude toward Learning in Ivano-Frankivsk National Medical University
- Role of Genetic Polymorphisms of the Renin-Angiotensin System and Immune Inflammation in the Development of Glycometabolic Disorders in Patients with Arterial Hypertension
- Influence of Metabolic Syndrome on Clinical Characteristics of Psoriasis
Last modified: 2016-03-15 03:09:11